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Medical Director Clinical Development Jobs in Basking Ridge, NJ

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Medical Director Clinical Development information

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$13.4K

$239.5K

$367.9K

How much do medical director clinical development jobs pay per year?

As of Aug 21, 2026, the average yearly pay for medical director clinical development in Basking Ridge, NJ is $239,469.00, according to ZipRecruiter salary data. Most workers in this role earn between $204,000.00 and $293,200.00 per year, depending on experience, location, and employer.

What does a medical director clinical development do?

A Medical Director of Clinical Development is responsible for overseeing the planning, execution, and management of clinical trials for new drugs or medical products. They work closely with cross-functional teams, such as regulatory affairs, clinical operations, and research scientists, to ensure that clinical studies are designed effectively and conducted in compliance with regulatory standards. Their role also includes reviewing and interpreting clinical data, providing medical expertise, and contributing to the overall strategy for product development. Medical Directors play a crucial role in ensuring the safety and efficacy of new therapies before they reach the market.

How does a medical director clinical development typically collaborate with cross-functional teams during a clinical trial?

As a Medical Director in Clinical Development, you will regularly collaborate with cross-functional teams such as clinical operations, regulatory affairs, biostatistics, data management, and pharmacovigilance. Your role involves providing medical and scientific guidance, ensuring protocol adherence, and addressing safety or efficacy concerns throughout the trial. Effective communication and teamwork are essential for aligning on trial objectives, managing timelines, and resolving any emerging issues. This collaborative environment fosters a comprehensive approach to advancing clinical programs and supports the successful execution of clinical trials.

What are the key skills and qualifications needed to thrive as a medical director clinical development, and why are they important?

To thrive as a Medical Director Clinical Development, you need an advanced medical degree (MD or equivalent), extensive clinical research experience, and a deep understanding of regulatory requirements and drug development processes. Familiarity with electronic data capture systems, clinical trial management software, and GCP/ICH guidelines is typically required. Strong leadership, strategic thinking, and exceptional communication skills help drive multidisciplinary teams and manage complex projects. These skills ensure the safe, efficient, and compliant progression of clinical programs from conception through regulatory approval.

What is the difference between Medical Director Clinical Development vs Medical Scientist?

AspectMedical Director Clinical DevelopmentMedical Scientist
Required CredentialsMD or DO, clinical research experience, industry certificationsMD, PhD, or equivalent, research-focused
Work EnvironmentPharmaceutical companies, biotech firms, clinical trial oversightResearch institutions, academia, laboratories
Employer & Industry UsageCommonly employed in industry to oversee clinical developmentPrimarily in research and academia, less in industry

The Medical Director Clinical Development typically oversees clinical trials and ensures regulatory compliance within the industry, requiring medical credentials and industry experience. Medical Scientists focus on research and discovery, often working in labs or academic settings. While both roles require advanced degrees, their work environments and primary responsibilities differ significantly.

What job categories do people searching Medical Director Clinical Development jobs in Basking Ridge, NJ look for?

The top searched job categories for Medical Director Clinical Development jobs in Basking Ridge, NJ are:

What cities near Basking Ridge, NJ are hiring for Medical Director Clinical Development jobs?

Cities near Basking Ridge, NJ with the most Medical Director Clinical Development job openings:

Medical Director Clinical Development jobs near you

Senior Director, Clinical Development

Initial Therapeutics, Inc.

Basking Ridge, NJ • On-site

$280.35 - $467.25/hr

Other

Posted 16 days ago

Job description

Job Description

Job Title: Senior Director, Clinical Development


Job Requisition ID: 1816


Posting Start Date: 7/15/26


At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.


Job Summary

The Senior Director sits within Global Oncology Clinical Development, an organization dedicated to the effective strategy, design, execution, and interpretation of Oncology clinical trials.


Position Summary / Objective

  • Serves as a primary source of medical accountability and oversight for one or more clinical trials

  • Matrix management responsibilities across the internal and external network

  • Manages Phase 1 - Phase 3 studies (depending on assignment) with demonstrated decision-making capabilities

  • Provides medical and scientific expertise to cross-functional DSI colleagues


Job Description
Responsibilities
Medical Monitoring

  • Provides medical input on study and country feasibility, including site feasibility assessments

  • Contributes to eCRF design, UAT, and CRF Completion Guidelines as needed

  • Conducts ongoing clinical data review and assesses protocol deviations

  • Addresses medical queries from sites/IRBs, including eligibility, safety, dose modifications, and adverse event management

  • Serves as study medical expert and oversees CRO Medical Monitor activities, including data review and medical guidance (e.g., AE coding)


Responsibilities Continued
Clinical Development Expertise & Strategy

  • Leads development and execution of the Clinical Development Plan (CDP), ensuring alignment with protocols and Target Product Profile (TPP)

  • Provides medical/scientific leadership for study design, protocol development, and key study-level documents (e.g., CSR, IB, regulatory responses)

  • Interprets and presents clinical data to internal and external stakeholders; supports regulatory and safety reporting (e.g., DSUR, PSUR)

  • Delivers scientific training and leads key study meetings (e.g., IM, SIV) on compound, disease, and safety management

  • Maintains deep therapeutic area expertise and contributes to strategic insights on disease landscape, competition, and product positioning (TPP/EPP)

  • Leads engagement with governance bodies (e.g., DMC, Steering Committee), including charter development, presentations, and ongoing oversight

  • Oversees external partnerships (e.g., CROs, AROs, cooperative groups) and contributes to labeling and product lifecycle management


Health Authority Interactions & Publications

  • May contribute to addressing questions about medical decisions, clinical data review, protocol deviations, etc., and/or scientific aspects of the study during FDA, MHRA, EMA, and PMDA interactions, such as pre-submissions, end of phase 1/2, and inspections

  • May support the GCL, if applicable, in planning and executing the overall publication and clinical communication strategy (overall or at the individual trial level), providing input to key external presentations.

  • Contributes to and serves as the medical point of expertise in key Health Authority interactions and Ad board meetings


Qualifications
Education Qualifications

  • MD required

  • Postgraduate training in TA or related specialty required


Experience Qualifications

  • 7 or more years relevant clinical experience required


Travel Requirements

Ability to travel up to 20% of the time. Domestic and International travel will be required.


Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.


Salary Range:


USD$280,350.00 - USD$467,250.00

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